paternal lineages

Related by string. paternal lineage * Paternal : Riley paternal grandmother . paternal grandfather . Semenya paternal grandmother . paternal ancestors . paternal affection . paternal grandparents . Paternal grandparents / Lineage : Assassin Creed Lineage . Embraer Lineage . ancestral lineage . distinct lineages . lineages diverged . illustrious lineage . lineage genealogy * *

Related by context. All words. (Click for frequent words.) 64 paternal ancestry 63 maternal lineages 63 genetic lineages 61 Y chromosomal 60 haplogroups 60 socioeconomic status SES 59 mitochondrial DNA mtDNA 58 dizygotic twins 58 paternal lineage 58 ancestries 58 allele frequencies 58 genetic ancestry 58 Homo sapiens evolved 58 haplotypes 57 APOE genotype 57 missense mutations 57 genomewide 57 MYH9 gene 57 germline mutations 57 monozygotic 56 MYH9 56 maternal lineage 56 genetic loci 56 outbred 56 chromosomal anomalies 56 chimp genomes 56 TGFBR1 * 6A 56 lactose tolerance 56 admixed populations 56 Ashkenazic Jews 56 Haplogroup 56 monozygotic twins 56 elevated serum ALT 56 proband 56 microbiomes 56 hominoids 56 sexually dimorphic 55 differentially expressed genes 55 telomere lengths 55 MLL2 55 paternally inherited 55 LPA gene 55 jawed vertebrates 55 mtDNA sequences 55 Single Nucleotide Polymorphisms 55 Mestizos 55 familial aggregation 55 de novo mutations 55 gene locus 55 familial clustering 55 microsatellite markers 55 Socioeconomic status 55 phenotypic characteristics 54 autosomal 54 chromosomal disorders 54 phylogenetic analyzes 54 microdeletions 54 genetically homogeneous 54 H. sapiens 54 TCF#L# gene 54 morphological traits 54 phenotypic variation 54 maternally inherited 54 BRCA2 mutations 54 Paranthropus robustus 54 susceptibility loci 54 DRD2 gene 54 colorectal neoplasia 54 ZNF# 54 heritable variation 54 Neanderthals interbred 54 tyrannosaurids 54 MLH1 54 landraces 54 internalizing disorders 54 Y Chromosome 53 BRCA1 mutations 53 Homo neanderthalensis 53 Comparative genomics 53 BARD1 53 Mitochondrial DNA 53 prehuman 53 central adiposity 53 epigenetic changes 53 hunter gatherer populations 53 subclinical atherosclerosis 53 orthologs 53 NPY gene 53 MC1R gene 53 methylation patterns 53 haplogroup 53 ancestry 53 nondemented 53 methylation markers 53 BRCA2 gene mutations 53 endophenotypes 53 choline intake 53 fetal aneuploidy 53 gestational diabetes mellitus 53 folate deficiency 53 #q# deletion 53 phylogeographic 53 prenatal phthalate exposure 53 congenital toxoplasmosis 53 quantitative trait loci 53 eusocial 53 mitochondrial Eve 53 miRNA expression 53 advanced neoplasia 53 A. ramidus 53 SRY gene 53 lactase persistence 53 Epidemiologic studies 53 Genetic variants 53 sequenced genomes 53 familial predisposition 53 BioMAP ® 53 epigenetic modifications 53 mitochondrial mutations 53 genetic markers 53 evolvability 53 microchimerism 53 perinatally infected 53 body louse genome 53 mtDNA 53 BRCA gene mutations 53 #S rRNA gene 53 chimpanzee genomes 53 allelic variation 53 GBA mutations 53 Ethnicities 53 prehistorical 53 #S rRNA 53 marsupial mammals 53 Emptying Nests 53 thrifty gene 53 matriarchal societies 53 DNA methylation patterns 52 homozygosity 52 VNTR 52 dizygotic 52 phylogenetically 52 Low birthweight 52 enterotypes 52 Neanderthal fossils 52 placental mammals 52 carotid plaque 52 apolipoprotein E gene 52 primate genomes 52 Nilo Saharan 52 haplotype map 52 hominin fossils 52 differential gene expression 52 Single Nucleotide Polymorphisms SNPs 52 clinicopathologic 52 susceptibility genes 52 Treponema pallidum 52 nonmarital births 52 breast cancer genes BRCA1 52 exponential regression 52 ribosomal RNA rRNA 52 Castorocauda 52 etiologic 52 Na Dene 52 sauropodomorphs 52 breast cancer subtypes 52 Telomere length 52 mitochondrial genome 52 ASD prevalence 52 sCJD 52 congenital CMV infection 52 Bos taurus 52 perinatal outcomes 52 genes BRCA1 52 transcriptomes 52 humans Homo sapiens 52 mutant allele 52 heritable traits 52 sporadic ALS 52 Nutrition EPIC 52 impaired glucose metabolism 52 genetic variants associated 52 gametophyte 52 gene variants 52 humans interbred 52 chimpanzees Pan troglodytes 52 KCNQ1 52 microscopic colitis 52 GABRA2 52 nucleotide substitutions 52 allergic sensitization 52 #q#.# deletion syndrome 52 Alleles 52 segmental duplications 52 serologic 52 sociodemographic 52 endogenous retroviruses 52 recombination hotspots 52 assortative mating 52 bilaterians 52 gene expression patterns 52 mitochondrial DNA lineages 52 body fatness 52 hunter gatherer societies 51 subclinical hyperthyroidism 51 autistic regression 51 vesper bats 51 Denisovan 51 adiponectin concentrations 51 repeat allele 51 syndromic 51 STK# gene 51 assortative 51 STAT4 51 microcephalin 51 hominoid 51 Neanderthal genes 51 phylogenetic relationships 51 HLA genes 51 previously undescribed 51 colorectal cancer incidence 51 Ashkenazi Jews 51 H. habilis 51 elevated CRP 51 QTLs 51 chromosome #q# [002] 51 somatic mutations 51 ornithischians 51 causal variants 51 multiple logistic regression 51 mtDNA mutations 51 BRCA mutations 51 mitochondrial genomes 51 Genetic profiling 51 ramidus 51 dietary intakes 51 confer susceptibility 51 CCR5 delta# 51 CYP#C# gene 51 socioeconomic characteristics 51 spontaneous mutations 51 Yamanaka recipe 51 Aramaic texts 51 bivariate 51 KRAS mutations 51 Cytogenetic 51 singleton babies 51 indel 51 metazoans 51 genetic polymorphisms 51 umbilical hernias 51 False killer whales 51 dbSNP 51 Multiple logistic regression 51 genotypic 51 CNTNAP2 51 serum leptin 51 phenotypic traits 51 breast cancer susceptibility genes 51 Plasmodium vivax 51 generalized vitiligo 51 Neanderthal skeletons 51 hominid species 51 chromosomal aberrations 51 mean ± SEM 51 MSH2 51 placental malaria 51 placentals 51 putative biomarkers 51 carotid plaques 51 hunter gatherer cultures 51 Thyroid nodules 51 KRAS BRAF 51 mitochondrial DNA 51 habilis 51 highly heritable 51 rs# [001] 51 loci 51 APOE ε4 51 genotyped 51 Boston DbTechNo Results 51 KCNH2 51 introgression 51 molecular abnormalities 51 Apobec3 51 inferential statistics 51 epistasis 51 familial pancreatic cancer 51 phenotypic differences 51 rs# [002] 51 Genetic variations 51 coronary revascularizations 51 pseudogenes 51 earliest hominid 51 CNVs 50 heterozygotes 50 Aspergillus nidulans 50 multigene 50 ENPP1 50 dietary patterns 50 paternal grandfathers 50 clinico pathological 50 hominid ancestors 50 trait locus 50 p# mutation 50 Gigantopithecus 50 microRNA expression 50 mitochondrial proteins 50 KIF6 gene 50 Genetic variation 50 animal phyla 50 genetic makeups 50 inherited mutations 50 hereditary hemochromatosis 50 Gestational 50 eusociality 50 biogeographical 50 acculturated Latinos 50 NLSY 50 CHD mortality 50 heritability 50 anthropoids 50 HLA DRB1 50 nongenetic 50 parous women 50 narcolepsy cataplexy 50 phenotypes 50 religiously unaffiliated 50 causative mutations 50 Methodists Lutherans 50 mtDNA sequence 50 HIV tropism 50 C#Y 50 epigenetic modification 50 Logistic regression 50 pelvic inlet 50 observable traits 50 cTnT 50 transcriptomics 50 chimpanzee Pan troglodytes 50 mule clones 50 species interbred 50 microdeletion 50 mutant alleles 50 Framingham Offspring 50 thalassemia trait 50 phenotypic expression 50 chromosomal alterations 50 sequence homology 50 KLF4 50 hantaviruses 50 Genetic Variation 50 homologies 50 Acculturation 50 sociodemographic factors 50 clefting 50 #p#.# [001] 50 Cucumis 50 Towering scholar 50 marital statuses 50 abnormal glucose tolerance 50 MHC genes 50 obesity sedentary lifestyle 50 socioeconomic deprivation 50 Afro descendants 50 ANCOVA 50 Haplotype 50 Olmec civilization 50 APOE e4 50 Mendelian disorders 50 inhibin B 50 thyroid hormone levels 50 orgins 50 prevalences 50 biogeographic 50 equids 50 Telomere shortening 50 metabolomic profiles 50 ORMDL3 50 amphioxus 50 promoter methylation 50 colugos 50 Homo antecessor 50 allelic variants 50 chromosome #p# [001] 50 patrilineal 50 NAFLD 50 prognostic markers 50 CDH1 50 hamartomas 50 monkeys apes 50 ancient hominids 50 causative genes 50 karyotypes 50 segmental duplication 50 ancestral lineage 50 Neanderthal extinction 50 HNPCC 50 CagA 49 CVD mortality 49 CHDs 49 PRNP 49 DRD4 49 HPV genotypes 49 karyotype 49 racial disparities persist 49 logistic regression analyzes 49 morphologically distinct 49 masculinization 49 Tsimane 49 Shorter telomeres 49 IPAH 49 Ashkenazi Jewish 49 linkage disequilibrium 49 autosomal recessive 49 seroprevalence 49 NHANES III 49 orthologous genes 49 faunas 49 Alu elements 49 cnidarians 49 BRAF V#E 49 KIBRA 49 menarche 49 genetically homogenous 49 HER2 expression 49 born preterm 49 S. sanguinis 49 genome rearrangements 49 eastern cougar subspecies 49 antenatal depression 49 chromosomal regions 49 ALK mutations 49 cytologic 49 hormone receptor status 49 phylogenies 49 dysbindin gene 49 Asperger syndrome Rett syndrome 49 genetic polymorphism 49 primate lineage 49 clade B 49 aneuploidies 49 CARDIA study 49 TCF#L# 49 Bulging bellies 49 genetic variations 49 genes differentially expressed 49 anthropometric measurements 49 genetic aberrations 49 organochlorine compounds 49 microalbumin 49 reassortants 49 mammographically 49 dopamine transporter gene 49 Negroid 49 #q# [001] 49 polygenic 49 CYP#D# gene 49 Male infertility 49 G6PD deficiency 49 chromosome #q# [001] 49 PTPN# 49 penetrance 49 miRNA sequences 49 lineages 49 Kadanuumuu 49 Y chromosomes 49 Transcriptome 49 Kushitic 49 UGT#B# 49 metabolic abnormalities 49 enamel defects 49 VKORC1 49 phylogenetic analysis 49 subsamples 49 monophyletic 49 Newschaffer 49 Netherlands Cohort Study 49 Fragile Families 49 Population Database 49 adenomatous polyps 49 serum lipid levels 49 genes CYP#C# 49 genetic susceptibility 49 HG PIN 49 ADH1B * 49 genomic proteomic 49 obese postmenopausal 49 susceptibility locus 49 denser breasts 49 gene DRD4 49 AVPR1A 49 KLF# gene 49 nones 49 genomic variation 49 genetically divergent 49 seropositivity 49 paternal discrepancy 49 T. vaginalis 49 colorectal carcinogenesis 49 Hadza 49 observational cohort study 49 hoofed mammals 49 phenotype 49 pipefish 49 moderately heritable 49 poor metabolizers 49 genus Homo 49 KRAS mutation 49 etiological 49 folate supplementation 49 parasitic flatworms 49 gastric carcinogenesis 49 PBDE concentrations 49 Pan troglodytes 49 singleton pregnancies 49 TACI mutations 49 2 diabetes T2D 49 genetic variation 49 imprinted genes 49 maternal serum 49 species Australopithecus afarensis 49 APOL1 49 Neandertal DNA 49 autosomes 49 extramedullary 49 Semitic peoples 49 Fragile X gene 49 monogenic diabetes 49 postnatally 49 animal herdmates 49 recessive inheritance 49 fungal genomes 49 artifactual 49 BRCA2 mutation carriers 49 homophily 49 anomodonts 49 primate cousins 49 mitochondrial disorders 49 earliest tetrapods 49 chromosome rearrangements 49 choanoflagellates 49 metazoan 49 Wisconsin Sleep Cohort 49 APOE e4 gene 49 Rh factor 49 IKZF1 49 GSTM1 49 atherothrombotic disease 49 FTO variant 49 allele frequency 49 MTHFR 49 diploid genome 49 parous 49 International HapMap Project 49 prion gene 49 microbiota 49 DQB1 * 49 Raptorex kriegsteini 49 visceral adiposity 49 Mitochondrial Eve 49 Colon polyps 49 Pierolapithecus 49 evolutionarily novel 49 cortex thickness 49 pathogenic mutations 49 Arabidopsis genome 49 SMGF database 49 morphological characteristics 49 Homo erectus fossils 49 chordate 49 fluoroquinolone resistant 48 multicentre prospective 48 A. thaliana 48 aortic calcification 48 perinatal morbidity 48 warm bloodedness 48 Bornean orangutans 48 #p# [001] 48 serological 48 firstborns 48 MC1R 48 distinct lineages 48 HIV HCV coinfected 48 genes predisposing 48 Hamitic 48 distinct subtypes 48 Selembu shows 48 testicular germ cell 48 Aztec Mayan 48 lymphoblastoid cell lines 48 allelic 48 chromosomal rearrangement 48 Rh incompatibility 48 genotype phenotype 48 GSTT1 48 ancestrally 48 ortholog 48 BRCA2 carriers 48 martian meteorites 48 Ardipithecus ramidus 48 cytochrome b 48 #q#.# [001] 48 multivariable Cox 48 Multiethnic Cohort Study 48 HSPCs 48 Descriptive statistics 48 NHANES #-# 48 chromosome deletion 48 Australopithecus genus 48 mitochondrial DNA sequence 48 Supplementary Table 48 adiposity 48 molecular phylogenetic 48 Natufian 48 genetic determinants 48 abnormal glucose metabolism 48 Surnames 48 intergenic 48 colorectal cancer CRC 48 Apolipoprotein E 48 chlamydial infection 48 vascular dysfunction 48 Multivariate analyzes 48 Isle Royale wolf 48 Univariate 48 sensu lato 48 CSF biomarkers 48 vermis 48 genomic variants 48 homologous genes 48 genetic variants 48 gene expression profiles 48 deCODE BreastCancer TM 48 Native Hawaiian Pacific Islander 48 Uto Aztecan 48 splice junctions 48 KIAA# 48 SE alleles 48 TT genotype 48 lipoprotein profile 48 gene duplications 48 socio demographic 48 Stegodon 48 HIES 48 gene APOE 48 insulin resistance syndrome 48 Dark skinned 48 major histocompatibility complex 48 Chlamydia trachomatis infection 48 Vitamin D supplementation 48 coding exons 48 chimps gorillas 48 epigenetic alterations 48 homo erectus 48 multiplex PCR 48 terrestrial vertebrates 48 indels 48 earlier Dorlean Nadege 48 Preterm births 48 genetic variability 48 fewer dopamine receptors 48 prepregnancy 48 Melungeons 48 hominid fossils 48 microbiologic 48 Australopithecus anamensis 48 H. erectus 48 gracile 48 Placental 48 Postpartum depression affects 48 southern supercontinent 48 orthologous 48 linkage disequilibrium LD 48 aY chromosome 48 IgA deficiency 48 #S ribosomal RNA 48 Univariate analysis 48 hereditary predisposition 48 Massospondylus 48 multigenerational households 48 mangabeys 48 serum selenium 48 Mariamene 48 ApoE gene 48 prehispanic 48 inbred strains 48 observational cohort 48 genital HPV infections 48 Insulin Sensitivity 48 phenotypically 48 genetic syndromes 48 DNA demethylation 48 endometrial cancers 48 transfusion syndrome 48 IgE antibody 48 tumor subtypes 48 KRAS variant 48 evolutionary lineage 48 aetiological 48 hemolytic diseases 48 perinatal mortality 48 carnivore species 48 Prevalence Estimates 48 retrospective cohort 48 carnivorous dinosaurs 48 prepregnancy BMI 48 KRAS oncogene 48 logistic regressions 48 chromosomal rearrangements 48 noncoding RNAs 48 genotypes 48 ethnically diverse populations 48 vertebrate embryos 48 gene polymorphisms 48 hemoglobins 48 mitochondrial genome sequence 48 heritable trait 48 ataxias 48 klotho 48 PALB2 48 ASCUS 48 APOE4 48 Study ARIC 48 nucleic acid sequence 48 genus Australopithecus 48 K ras gene 48 Multi Ethnic Study 48 Coronary artery calcification 48 #q# [002] 48 Polycystic ovarian syndrome 48 atopy 48 genomewide association studies 48 polyploid 48 causative mutation 48 P. falciparum malaria 48 Chicanas 48 genetically mapped 48 sociodemographic characteristics 48 CYP#D# genotype 48 genital abnormalities 48 ABCB1 gene 48 australopithecines 48 aneuploid cells 48 BMI percentiles 48 consanguineous marriage 48 Zapotecs 48 splice variants 48 CHRNA5 gene 48 Sahelanthropus 48 Cardiac Allograft Rejection 48 stepwise logistic regression 48 medulloblastomas 48 NAT2 48 susceptibility gene 48 modifier genes 48 limiting generalizability 48 fetal nucleic acids 48 ancient Phoenicians 48 socioeconomic variables 48 autosomal recessive disease 48 NorStates Bank serves 48 K ras 48 longitudinal studies 48 variant rs# 48 arterial thickening 48 H. heidelbergensis 48 lignan intake 48 ELISpot 48 positional cloning 48 amyloid cascade 48 Felis silvestris 48 histone modifications 48 Gestational age 48 embryonal 48 Darwin finches 48 mammal fossils 48 hypermethylated 48 nonfasting triglyceride levels 48 autosomal dominant inheritance 48 delaying childbearing 48 Salk scientists 48 oral cleft 48 hydroxyvitamin D levels 48 breast carcinomas 48 apoE 48 carbohydrate intolerance 48 SLITRK1 48 shorter telomere length 48 autistic traits 48 ostriches emus 48 TP# gene 48 anal HPV 48 rs# [003] 48 LRP5 48 prenatally diagnosed 48 HLA gene 48 Interview Survey CHIS 48 species Homo floresiensis 48 studies GWAS 48 Preterm delivery 48 genotype 48 bone density measurements 48 tau protein tangles 48 Neandertal 48 mulattoes 48 mammary gland tumors 48 Avon Longitudinal Study 48 onset diabetes mellitus 48 S. maltophilia 48 dietary fiber intake 48 masculine traits 48 plasma lipid 48 paternal ancestor 48 Chlamydia pneumoniae 48 chromosome #p# [002] 48 viral etiology 48 Unwed mothers 48 beta carotene supplementation 48 mammalian genomes 48 TP# mutation 48 perilipin 48 heritable 47 hominin species 47 microsatellite instability 47 Prevotella 47 molecular phylogeny 47 woolly rhinoceros 47 Bacteroides 47 fraternal twin pairs 47 NNRTI resistance 47 VLBW 47 bile acid metabolism 47 ELBW infants 47 Homo species 47 facial clefts 47 Quova delivers 47 T2D 47 neotropical 47 defining interracial marriages 47 PIK3CA 47 psychographic profile 47 Ancient Macedonians 47 taxa 47 maternally transmitted 47 elevated triglyceride levels 47 neuroblastomas 47 generalisable 47 K ras mutations 47 HIV serostatus 47 obesity insulin resistance 47 BRCA2 mutation 47 H. pylori infections 47 CYP#A# gene 47 CpG island 47 socioeconomic inequalities 47 gut microbes 47 colorectal adenomas 47 ependymomas 47 fluoroquinolone resistance 47 chromatin immunoprecipitation ChIP 47 heritable diseases 47 Genetic testing 47 tlee 47 wild canids 47 genetic variant 47 hominins 47 nicotine metabolite 47 thicker carotid arteries 47 ape ancestors 47 Dietary habits 47 prostate carcinogenesis 47 Depressive disorders afflict 47 polyandrous 47 preterm deliveries 47 periprocedural MI 47 Australopithecines 47 during conception Giwercman 47 Venter genome 47 taxon 47 SORT OUT III 47 heritable disorders 47 haplotype 47 serum biomarkers 47 commonly mutated genes 47 bioinformatic approaches 47 monogenic 47 sexual dimorphism 47 artiodactyls 47 pool dies unwept 47 nonidentical twins 47 BMPR2 47 heterozygous 47 FGFs 47 Pygmy hippos 47 postmenopausal hormone 47 Haptoglobin 47 aneuploid 47 Homo ergaster 47 Alternative splicing 47 probands 47 phenotypic variability 47 teosinte 47 perinatally 47 endangered subspecies 47 heritable component 47 Basal cell carcinomas 47 CC genotype 47 dopamine receptor gene 47 Chlamydia trachomatis 47 immunochemical 47 Y STR 47 leptin resistant 47 MicroRNA 47 Mesoamerican cultures 47 RhD 47 HLA DQ2 47 intestinal biopsy 47 Related Conditions NESARC 47 Birth Weight 47 fetal chromosomal abnormalities 47 SNPs 47 CHAMACOS 47 Eurasians 47 RBP4 47 Makovicky 47 molecular systematics 47 transcriptome profiling 47 toxicogenomic 47 exomes 47 Wwox 47 vasopressin receptors 47 glowing piglets 47 alleles 47 thrombophilia 47 mutated genes 47 genetic heterogeneity 47 ultra rapid metabolizer 47 Genetic predisposition 47 corticosterone levels 47 shorter lifespans 47 SLC#A# gene [001] 47 hominid evolution 47 Sporadic CJD 47 Hypertensive heart 47 mosaicism 47 genomic alterations 47 Epidemiological studies 47 anti JCV antibodies 47 mRNA transcripts 47 obstructive coronary artery 47 chromosome #q#.# [001] 47 recessive trait 47 proteomes 47 ambivalent networkers 47 Censuses 47 BRCA carriers 47 epigenetic markers 47 Acute lymphoblastic leukemia 47 FMR1 47 nucleotide sequence 47 subfamilies 47 molecular subtypes 47 nondiabetic 47 Evidence Therapeutic study 47 BRIP1 47 intersexuality 47 aneuploidy screening 47 Female infanticide 47 BRCA1 mutation carriers 47 eukaryote 47 Linear regression 47 Mixtecs 47 cytogenetic 47 underlying pathophysiology 47 colonoscopy sigmoidoscopy 47 #S rDNA 47 HGPS 47 evolutionary divergence 47 MHC dissimilar 47 microcephalics 47 H. floresiensis 47 epistatic 47 Afro descendent 47 chromosome aberrations 47 potentially modifiable 47 SCN5A 47 serum retinol 47 Asians Middle Easterners 47 immunochemical fecal occult 47 Aggressive Prostate Cancer 47 thimerosal exposure 47 ethno linguistic groups 47 morphological similarities 47 neural underpinnings 47 salivary proteins 47 asexuals 47 androgen deficiency 47 NPM1 gene

Back to home page